Biogenesis of Tom40, core component of the TOM complex of mitochondria.
Tom40 is an essential component of the preprotein translocase of the mitochondrial outer membrane (TOM complex) in which it constitutes the core element of the protein conducting pore. We have investigated the biogenesis of Tom40. Tom40 is inserted into the outer membrane by the TOM complex. Initially, Tom40 is bound ... as a monomer at the mitochondrial surface. The import receptor Tom20 is involved in this initial step; it stimulates both binding and efficient insertion of the Tom40 precursor. This step is followed by the formation of a further intermediate at which the Tom40 precursor is partially inserted into the outer membrane. Finally, Tom40 is integrated into preexisting TOM complexes. Efficient import appears to require the Tom40 precursor to be in a partially folded conformation. Neither the NH(2) nor the COOH termini are necessary to target Tom40 to the outer membrane. However, the NH(2)-terminal segment is required for Tom40 to become assembled into the TOM complex. A model for the biogenesis of Tom40 is presented.
Mesh Terms:
Biological Transport, Cross-Linking Reagents, Endopeptidases, Intracellular Membranes, Kinetics, Membrane Proteins, Membrane Transport Proteins, Mitochondria, Mitochondrial Membrane Transport Proteins, Models, Biological, Molecular Weight, Multienzyme Complexes, Neurospora crassa, Peptide Fragments, Protein Binding, Protein Conformation, Protein Denaturation, Protein Folding, Protein Precursors, Protein Processing, Post-Translational, Protein Sorting Signals, Receptors, Cytoplasmic and Nuclear, Saccharomyces cerevisiae Proteins, Sequence Deletion, Temperature
Biological Transport, Cross-Linking Reagents, Endopeptidases, Intracellular Membranes, Kinetics, Membrane Proteins, Membrane Transport Proteins, Mitochondria, Mitochondrial Membrane Transport Proteins, Models, Biological, Molecular Weight, Multienzyme Complexes, Neurospora crassa, Peptide Fragments, Protein Binding, Protein Conformation, Protein Denaturation, Protein Folding, Protein Precursors, Protein Processing, Post-Translational, Protein Sorting Signals, Receptors, Cytoplasmic and Nuclear, Saccharomyces cerevisiae Proteins, Sequence Deletion, Temperature
J. Cell Biol.
Date: Jul. 26, 1999
PubMed ID: 10427088
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